Primary Device ID | 08809702401762 |
NIH Device Record Key | bc4fc6f5-18d2-4c7c-9055-0d5a90021d49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KJ Mini Implant System |
Version Model Number | MIPR5008-25 |
Company DUNS | 688476027 |
Company Name | KJMEDITECH.CO.,LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809702401762 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2019-11-19 |
08809702404534 | KJ Mini Implant System/Post Abutment |
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